Canonical Allele Identifier: CA2180843917
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs985575234

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419406T>C , CM000677.2:g.59419406T>C GRCh38
NC_000015.9:g.59711605T>C , CM000677.1:g.59711605T>C GRCh37
NC_000015.8:g.57498897T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000558348.5:c.-78+17048T>C ENSP00000453918.1:n.-78+17048T>C
ENST00000560394.5:c.-78+17048T>C ENSP00000452962.1:n.-78+17048T>C
XM_006720399.1:c.-78+17048T>C XP_006720462.1:n.-78+17048T>C
XM_011521248.1:c.-22+17048T>C XP_011519550.1:n.-22+17048T>C
XM_011521248.2:c.-22+17048T>C XP_011519550.1:n.-22+17048T>C